NDC 71335-0456-00 - Diclofenac Sodium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 71335-0456
- Requested NDC
- 71335-0456-00
- Package NDCs from labels
- 71335-0456-3, 71335-0456-9, 71335-0456-6, 71335-0456-0, 71335-0456-1, 71335-0456-7, 71335-0456-4, 71335-0456-2, 71335-0456-8, 71335-0456-5, 71335-0456-00
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2025-03-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diclofenac Sodium - Bryant Ranch Prepack | Bryant Ranch Prepack | 2025-03-28 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-0456-0 | Diclofenac Sodium | 40 in 1 BOTTLE | TABLET, DELAYED RELEASE | 40 | 5 | |
| 71335-0456-1 | Diclofenac Sodium | 28 in 1 BOTTLE | TABLET, DELAYED RELEASE | 28 | 5 | |
| 71335-0456-2 | Diclofenac Sodium | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | 5 | |
| 71335-0456-3 | Diclofenac Sodium | 20 in 1 BOTTLE | TABLET, DELAYED RELEASE | 20 | 5 | |
| 71335-0456-4 | Diclofenac Sodium | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | 5 | |
| 71335-0456-5 | Diclofenac Sodium | 120 in 1 BOTTLE | TABLET, DELAYED RELEASE | 120 | 5 | |
| 71335-0456-6 | Diclofenac Sodium | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | 5 | |
| 71335-0456-7 | Diclofenac Sodium | 100 in 1 BOTTLE | TABLET, DELAYED RELEASE | 100 | 5 | |
| 71335-0456-8 | Diclofenac Sodium | 15 in 1 BOTTLE | TABLET, DELAYED RELEASE | 15 | 5 | |
| 71335-0456-9 | Diclofenac Sodium | 14 in 1 BOTTLE | TABLET, DELAYED RELEASE | 14 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-0456 | DICLOFENAC SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK] | 5 | Current NDC, Legacy NDC, 10 package rows | 20250331_487fa223-f4d9-4ab1-a5af-fb0d93f2bd0e.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-0456-0 | EA - Each | 71335-0456 | 8edd1a66-bc54-46d3-9d9d-662f0f0db6aa | 1 | 2018-03-08 |
| 71335-0456-1 | EA - Each | 71335-0456 | 27f9c6c0-3463-4d15-a5b0-88c198ac3709 | 1 | 2018-03-08 |
| 71335-0456-2 | EA - Each | 71335-0456 | 1ef18911-3049-45f1-99b4-2888c5b2cf3e | 1 | 2018-03-08 |
| 71335-0456-3 | EA - Each | 71335-0456 | b1be1f32-7f2c-4a6a-98f9-e4a6665e0522 | 1 | 2018-03-08 |
| 71335-0456-4 | EA - Each | 71335-0456 | ffbe2a00-69d8-4cea-98f5-bb8be0abcbd2 | 1 | 2018-03-08 |
| 71335-0456-5 | EA - Each | 71335-0456 | 1e493354-7953-4edd-9a6e-9822a8ef0a25 | 1 | 2018-03-08 |
| 71335-0456-6 | EA - Each | 71335-0456 | 2b96d76f-ae96-436b-aa7f-8bd545d00726 | 1 | 2018-03-08 |
| 71335-0456-7 | EA - Each | 71335-0456 | 43499d56-6e1c-47d1-8113-65176f352b5b | 1 | 2018-03-08 |
| 71335-0456-8 | EA - Each | 71335-0456 | b5aaba6e-f5da-42a5-88c3-2991f3492b14 | 1 | 2018-03-08 |
| 71335-0456-9 | EA - Each | 71335-0456 | 76557782-b50e-4a75-a64f-aff7e30bb359 | 1 | 2018-03-08 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | W Aesthetics | 5b0f2c8f-d6fa-5e25-e063-6394a90a084d | 2026-09-09 | Warnings | 15FIX9V2JP |
| Leader Artificial Tears 15 mL | POLYVINYL ALCOHOL, POVIDONE | Cardinal Health | 8cccc589-3a8e-baad-e053-2a95a90ab8c7 | 2026-09-09 | Warnings | FZ989GH94E |
| Calamine | CALAMINE, PRAMOXINE HCL | United Natural Foods, Inc. dba UNFI | 0bc1a9b4-1210-4d9a-bbd2-40e9225e86ea | 2026-09-04 | Warnings, Adverse reactions | 1K09F3G675 |
| FRESHKOTE PRESERVATIVE FREE LUBRICANT EYE DROPS | POVIDONE, POLYVINYL ALCOHOL SOLUTION | Harrow Eye, LLC | 049e9cc9-0663-53bc-e063-6294a90a2c4f | 2026-09-04 | Warnings | FZ989GH94E |
| Diclofenac Sodium | DICLOFENAC SODIUM | A-S Medication Solutions | d9698809-4887-4514-aa28-0066355ef908 | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | NuCare Pharmaceuticals, Inc. | 5a852412-69af-6502-e063-6294a90a0748 | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | 855906 QTG126297Q |
| Diclofenac | DICLOFENAC SODIUM | YYBA CORP | 533653e8-93d5-9080-e063-6394a90a165b | 2026-09-01 | Warnings | QTG126297Q |
| Diclofenac sodium and Misoprostol | DICLOFENAC SODIUM AND MISOPROSTOL | Mylan Pharmaceuticals Inc. | a7701e8c-4e16-4165-8b83-de2c08d5ded3 | 2026-08-31 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Diclofenac Sodium and Misoprostol | DICLOFENAC SODIUM AND MISOPROSTOL | Actavis Pharma, Inc. | df8b8660-0c24-4848-8bea-c1b935090c66 | 2026-08-31 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Calamine | FERRIC OXIDE RED | Your Military Exchanges | af95a66c-f063-4019-80c6-6f7dc4fee4d8 | 2026-08-28 | Warnings, Adverse reactions | 1K09F3G675 |
| MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50 | SUNSCREEN SPF50 | Guangzhou Meixi Biotechnology Co., Ltd. | 5a0b4bd2-f6ad-35dc-e063-6294a90a8a66 | 2026-08-27 | Warnings | 15FIX9V2JP |
| MELAO Hydrating Lightweight Sunscreen | AVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDE | Guangdong Aimu Biological Technology Co., Ltd | 59eeaea1-d726-99f3-e063-6394a90aeea3 | 2026-08-26 | Warnings | 15FIX9V2JP |
| Calamine Plus | CALAMINE, PRAMOXINE HYDROCHLORIDE | Kroger Company | 44fdd5a4-3cac-15e5-e063-6294a90adb52 | 2026-08-26 | Warnings | 1K09F3G675 |
| Q Skin Science | SUNSCREEN | International Cosmeceuticals, Inc | 59e4c3d0-ee4c-2350-e063-6394a90ac9d2 | 2026-08-25 | Warnings | 15FIX9V2JP |
| MELAO zinc stick(GREEN) | TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENE | Guangzhou Haishi Biological Technology Co., Ltd. | 59c70c82-f7ff-9a04-e063-6294a90a7b3d | 2026-08-24 | Warnings | 15FIX9V2JP |
| SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01 | ZINC OXIDE, TITANIUM DIOXIDE | Cosmuses Cosmetics (Ningbo) Co., Ltd. | 59d74e3f-e3fa-a7a9-e063-6294a90a76e5 | 2026-08-24 | Warnings | 15FIX9V2JP |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | Northwind Health Company, LLC | 5990259d-2f90-20d3-e063-6394a90a3d23 | 2026-08-21 | Boxed warning, Warnings, Adverse reactions | 855926 QTG126297Q |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | FZ989GH94E |
| Rohto All-In-One | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE | The Mentholatum Company | 43e690e4-b381-46e3-838c-33aef5bdadde | 2026-08-20 | Warnings | 3NXW29V3WO |
| Sweat Resistant Sunscreen Body Original | TITANIUM DIOXIDE, ZINC OXIDE | Clutch, Inc. | 4bbde755-e312-123e-e063-6294a90a467f | 2026-08-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.